Results 1 to 10 of about 94,996 (311)
Langerhans cell histiocytosis [PDF]
São Paulo Medical Journal, 1998 The authors present a rare case of Langerhans cell histiocytosis in a 31 year old female patient with vulvar, peri-anal and oral lesions, diabetes insipidus, pulmonary skin and bone infiltrations.
Maria de Lourdes L. F. Chauffaille +10 more
doaj +9 more sources
Langerhans‐Cell Histiocytosis [PDF]
Indian Journal of Medical Research, 2018 Langerhans cell histiocytosis (LCH) formerly known as pulmonary eosinophilic granuloma is currently regarded by the World Health Organization as a clonal neoplastic proliferation of histiocytes.
C. Allen, M. Merad, K. McClain
semanticscholar +6 more sources
Langerhans Cell histiocytosis. [PDF]
Blood, 2020 Langerhans Cell Histiocytosis (LCH) is caused by clonal expansion of myeloid precursors that differentiate into CD1a+/CD207+ cells in lesions that leads to a spectrum of organ involvement and dysfunction.
C. Rodríguez-Galindo, C. Allen
semanticscholar +4 more sources
Langerhans Cell Histiocytosis [PDF]
Dermatology Online Journal, 2002 Adult onset Langerhans cell histiocytosis is uncommon. A 29 year old man is presented who developed classic cutaneous disease with severe systemic involvement. He responded completely to a two month course of thalidomide.
Geraldine S. Pinkus +5 more
openalex +4 more sources
Beyond BRAF<sup>V600E</sup>: Investigating the Clinical and Genetic Spectrum of Langerhans Cell Histiocytosis in Children. [PDF]
Cancer MedABSTRACT Background Langerhans cell histiocytosis (LCH) is the most prevalent histiocytic disorder in pediatric populations, with a highly heterogeneous clinical presentation. Currently, the correlation between clinical phenotypes and molecular alterations in childhood LCH, besides the BRAFV600E mutation, has not been sufficiently studied. Methods This
Tang X, Gao J, Guo X, Wan Z, Sun JJ.
europepmc +2 more sources
Dynamic endoscopic progression of gastrointestinal tract involvement in Langerhans cell histiocytosis: A pediatric case report. [PDF]
DEN OpenAbstract Gastrointestinal tract involvement in Langerhans cell histiocytosis (LCH) is extremely rare, with limited documentation of endoscopic manifestations. We report a 19‐month‐old girl who presented with repeated diarrhea and bloody stools, accompanied by recurrent pulmonary infections, anemia, hypoproteinemia, thrombocytopenia, coagulopathy, and ...
Pan J, Liu B, Zhang H, Li Z.
europepmc +2 more sources
Langerhans' cell histiocytosis in adults [PDF]
Journal of the American Academy of Dermatology, 1997 Three cases of Langerhans' cell histiocytosis with unusual clinical and histopathologic features are described. The first two cases illustrate diagnostic pitfalls that underscore the importance of considering Langerhans' cell histiocytosis in the differential diagnosis of purpuric papular eruptions of the scalp and intertriginous areas, particularly in
Fiorina Giona +9 more
openalex +4 more sources
Клинический разбор в общей медицине, 2023 Langerhans cell histiocytosis is a rare proliferative disease of histiocyte-like cells, the peak incidence of which occurs in early childhood. Pulmonary Langerhans Cell Histiocytosis is one of the forms of this disease, but it usually affects young ...
Victor V. Fomin +4 more
doaj +2 more sources
Differentiation of Langerhans cells in Langerhans cell histiocytosis [PDF]
Blood, 2001 Langerhans cell histiocytosis (LCH) consists of lesions composed of cells with a dendritic Langerhans cell (LC) phenotype. The clinical course of LCH ranges from spontaneous resolution to a chronic and sometimes lethal disease. We studied 25 patients with various clinical forms of the disease.
Frédéric Geissmann +8 more
openalex +4 more sources
Langerhans cell histiocytosis [PDF]
British Journal of Haematology, 2000 Richard D. Brunning
openalex +4 more sources